Showing results (21-30 of 255) with videos related to
Sort By:
Pageof 26
Clinical Genetics|September 1, 1980
Pitfalls in the prenatal diagnosis of propionic acidemiaP D Buchanan, S G Kahler, L Sweetman, et al.The Journal of Pediatrics|May 1, 1975
Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosisW B Wadlington, A Kilroy, T Ando, et al.JAMA|September 7, 1979
Prenatal diagnosis of propionic acidemiaL Sweetman, W Weyler, T Shafai, et al.Pediatric Research|January 1, 1990
Effect of lipoic acid in a patient with defective activity of pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase, and branched-chain keto acid dehydrogenaseI Yoshida, L Sweetman, S Kulovich, et al.Pediatrics|October 1, 1981
Clinical and metabolic abnormalities in a boy with dietary deficiency of biotinL Sweetman, L Surh, H Baker, et al.Journal of Inherited Metabolic Disease|January 1, 1980
Propionic acidaemia presenting with pancytopaenia in infancyL Sweetman, W L Nyhan, J Cravens, et al.Pediatric Research|October 1, 1991
3-Hydroxyisobutyric aciduria: an inborn error of valine metabolismF J Ko, W L Nyhan, J Wolff, et al.American Journal of Diseases of Children (1960)|December 1, 1992
An unusual presentation of medium-chain acyl coenzyme A dehydrogenase deficiencyD Marsden, K Sege-Petersen, W L Nyhan, et al.Journal of Inherited Metabolic Disease|January 1, 1989
Methylcitrate in maternal urine during a pregnancy with a fetus affected with propionic acidaemiaS Aramaki, D Lehotay, W L Nyhan, et al.European Journal of Pediatrics|September 1, 1984
Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduriaK M Gibson, L Sweetman, W L Nyhan, et al.Pageof 26